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Antral Follicle Priming Prior to ICSI (Intracytoplasmic Sperm Injection) in Previously Diagnosed Low Responders (FOLLPRIM)

Primary Purpose

Ovarian Diseases

Status
Completed
Phase
Phase 2
Locations
Spain
Study Type
Interventional
Intervention
Testosterone
Estradiol
CombEq
Sponsored by
Instituto de Investigacion Sanitaria La Fe
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ovarian Diseases focused on measuring estradiol, testosterone, combined oral contraceptive, low responders, ICSI

Eligibility Criteria

18 Years - 41 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Phase 1 (Non randomized. The patient must fit the first plus at least other 2 criteria)

    • Infertility requiring an IVF/ICSI treatment
    • Age ≥ 38 years
    • Basal FSH ≥ 10 mUI/ml (day 3 of the cycle)
    • Serum AMH ≤ 5 pmol/l
    • Antral follicular count ≤ 6 (day 3 of the cycle)
  2. Phase 2 (Randomized. The patient must fit at least one criterion regarding the day of GNRH analogue administration during the cycle performed in Phase 1)

    • Less than 4 follicles which mean diameter measuring more than 16mm
    • Serum estradiol levels ≤ 500 pg/ml
    • 4 MII or less than 4 MII oocytes retrieved

Exclusion Criteria:

  • Patients suffering of endometriosis
  • Patients having progesterone levels ≤ 4 ng/ml (day 21 of the cycle)
  • Patients having a partner affected by severe oligo/astheno/teratozoospermia

Sites / Locations

  • La Fe University Hospital. Department of Obstetrics and Gynecology

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Testosterone

Estradiol

CombEq

Arm Description

Transdermal testosterone (20µg/day) from day 24 of the previous cycle until day 2 of the ICSI cycle

Transdermal estradiol (200µg/day)from day 20 of the previous cycle to day 3 of the ICSI cycle

(150µg Desogestrel + 30µg Ethinylestradiol)/day during the luteal phase of the two cycles prior to the ICSI Estradiol valerate 4 mg/day during 10 days, starting the second day of the cycle prior to the ICSI cycle.

Outcomes

Primary Outcome Measures

Number of MII oocytes retrieved

Secondary Outcome Measures

Total number of follicles punctured
Total number of oocytes retrieved
Total number of viable embryos
Serum and Follicular hormonal levels (testosterone, androstenedione, estradiol)
Granulosa cells genetic expression profile
Implantation rate
Pregnancy rate
Clinical pregnancy rate

Full Information

First Posted
March 7, 2011
Last Updated
February 27, 2014
Sponsor
Instituto de Investigacion Sanitaria La Fe
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1. Study Identification

Unique Protocol Identification Number
NCT01310647
Brief Title
Antral Follicle Priming Prior to ICSI (Intracytoplasmic Sperm Injection) in Previously Diagnosed Low Responders
Acronym
FOLLPRIM
Official Title
Prospective Randomized Controlled Trial of Antral Follicle Priming Prior to IVF-ICSI in Previously Diagnosed Low Responders.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2014
Overall Recruitment Status
Completed
Study Start Date
June 2011 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
February 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Instituto de Investigacion Sanitaria La Fe

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to compare the effectiveness of testosterone,estradiol and a combined treatment with estrogens/progestagens prior to IVF-ICSI in previously diagnosed low responder patients.
Detailed Description
During controlled ovarian hyperstimulation (COH), most of the early antral follicles are required to grow coordinately. Marked follicular size discrepancies during COH imply that an important number of follicles undergo unsatisfactory maturation. It has been proved that follicular priming with estradiol during the luteal phase of the cycle prior to COH or testosterone treatment during the early follicular phase of the COH cycle may increase the amount of oocytes and embryos retrieved. Nevertheless there are no prospective studies comparing such approaches. The present study consist of two phases: The present study consists of two different phases: Phase I: (Non randomized) Identification of confirmed low responder patients. Potential low responder patients will be subjected to an standardized ovarian hyperstimulation protocol Phase II: (Randomized) those patients, once confirmed as low responders, will be offered the opportunity to enter the interventional part of the study, being randomized to three different treatment groups: estradiol, testosterone or combined progestagens and estrogens prior to the IVF-ICSI cycle. The previous cycle (phase I) will be used as a self-control for each patient.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ovarian Diseases
Keywords
estradiol, testosterone, combined oral contraceptive, low responders, ICSI

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
66 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Testosterone
Arm Type
Experimental
Arm Description
Transdermal testosterone (20µg/day) from day 24 of the previous cycle until day 2 of the ICSI cycle
Arm Title
Estradiol
Arm Type
Experimental
Arm Description
Transdermal estradiol (200µg/day)from day 20 of the previous cycle to day 3 of the ICSI cycle
Arm Title
CombEq
Arm Type
Experimental
Arm Description
(150µg Desogestrel + 30µg Ethinylestradiol)/day during the luteal phase of the two cycles prior to the ICSI Estradiol valerate 4 mg/day during 10 days, starting the second day of the cycle prior to the ICSI cycle.
Intervention Type
Drug
Intervention Name(s)
Testosterone
Other Intervention Name(s)
Testopatch, Pierre Fabre Ibérica S.A.
Intervention Description
Transdermal testosterone (20µg/kg/day)from day 24 of the previous cycle to day 2 of the ICSI cycle
Intervention Type
Drug
Intervention Name(s)
Estradiol
Other Intervention Name(s)
Alcis 100, Chiesi España
Intervention Description
Transdermal estradiol (200µg/day)from day 20 of the previous cycle to day 3 of the ICSI cycle
Intervention Type
Drug
Intervention Name(s)
CombEq
Other Intervention Name(s)
Microdiol, MERCK SHARP & DOHME, Meriestra 2mg, Novartis Farmacéutica, S.A.
Intervention Description
(150µg Desogestrel + 30µg Ethinylestradiol)/day during the luteal phase of the two cycles prior to the ICSI. Valerate estradiol 4mg/day during 10 days, starting the second day of the cycle prios to the ICSI cycle.
Primary Outcome Measure Information:
Title
Number of MII oocytes retrieved
Time Frame
36h after GnRH analogue administration
Secondary Outcome Measure Information:
Title
Total number of follicles punctured
Time Frame
36h after GnRH analogue administration
Title
Total number of oocytes retrieved
Time Frame
36h after GnRH analogue administration
Title
Total number of viable embryos
Time Frame
48h after follicular puncture
Title
Serum and Follicular hormonal levels (testosterone, androstenedione, estradiol)
Time Frame
36h after GnRH analogue administration
Title
Granulosa cells genetic expression profile
Time Frame
36h after GnRH analogue administration
Title
Implantation rate
Time Frame
15 days after embryo transfer
Title
Pregnancy rate
Time Frame
15 days after embryo transfer
Title
Clinical pregnancy rate
Time Frame
5 weeks after embryo transfer

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
41 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Phase 1 (Non randomized. The patient must fit the first plus at least other 2 criteria) Infertility requiring an IVF/ICSI treatment Age ≥ 38 years Basal FSH ≥ 10 mUI/ml (day 3 of the cycle) Serum AMH ≤ 5 pmol/l Antral follicular count ≤ 6 (day 3 of the cycle) Phase 2 (Randomized. The patient must fit at least one criterion regarding the day of GNRH analogue administration during the cycle performed in Phase 1) Less than 4 follicles which mean diameter measuring more than 16mm Serum estradiol levels ≤ 500 pg/ml 4 MII or less than 4 MII oocytes retrieved Exclusion Criteria: Patients suffering of endometriosis Patients having progesterone levels ≤ 4 ng/ml (day 21 of the cycle) Patients having a partner affected by severe oligo/astheno/teratozoospermia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
César Díaz, M.D.
Organizational Affiliation
La Fe University Hospital. Department of Obstetrics and Gynecology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Antonio Pellicer, Professor
Organizational Affiliation
La Fe University Hospital. Department of Obstetrics and Gynecology
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Alicia Marzal, M.D.
Organizational Affiliation
La Fe University Hospital. Department of Obstetrics and Gynecology
Official's Role
Study Chair
Facility Information:
Facility Name
La Fe University Hospital. Department of Obstetrics and Gynecology
City
Valencia
ZIP/Postal Code
46026
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
14645194
Citation
Fanchin R, Salomon L, Castelo-Branco A, Olivennes F, Frydman N, Frydman R. Luteal estradiol pre-treatment coordinates follicular growth during controlled ovarian hyperstimulation with GnRH antagonists. Hum Reprod. 2003 Dec;18(12):2698-703. doi: 10.1093/humrep/deg516.
Results Reference
background
PubMed Identifier
19054777
Citation
Fabregues F, Penarrubia J, Creus M, Manau D, Casals G, Carmona F, Balasch J. Transdermal testosterone may improve ovarian response to gonadotrophins in low-responder IVF patients: a randomized, clinical trial. Hum Reprod. 2009 Feb;24(2):349-59. doi: 10.1093/humrep/den428. Epub 2008 Dec 3.
Results Reference
background
PubMed Identifier
25955224
Citation
Escriva AM, Diaz-Garcia C, Monterde M, Rubio JM, Pellicer A. Antral Follicle Priming Before Intracytoplasmic Sperm Injection in Previously Diagnosed Low Responders: A Randomized Controlled Trial (FOLLPRIM). J Clin Endocrinol Metab. 2015 Jul;100(7):2597-605. doi: 10.1210/jc.2015-1194. Epub 2015 May 8.
Results Reference
derived

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Antral Follicle Priming Prior to ICSI (Intracytoplasmic Sperm Injection) in Previously Diagnosed Low Responders

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